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N-[1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-2-methylpropyl]-2,4-dimethoxybenzenesulfonamide | 1131730-48-7

中文名称
——
中文别名
——
英文名称
N-[1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-2-methylpropyl]-2,4-dimethoxybenzenesulfonamide
英文别名
——
N-[1-(5,8-dihydroxy-1,4-dioxonaphthalen-2-yl)-2-methylpropyl]-2,4-dimethoxybenzenesulfonamide化学式
CAS
1131730-48-7
化学式
C22H23NO8S
mdl
——
分子量
461.493
InChiKey
DNYUENVYYHCFTP-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.6
  • 重原子数:
    32
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    148
  • 氢给体数:
    3
  • 氢受体数:
    9

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis and biological activity of novel shikonin analogues
    摘要:
    A series of shikonin analogues with side chain variants have been synthesized and evaluated for antitumor activity. These novel analogues show a broad spectrum of in vitro cytotoxicity against various cancer cell lines. Additionally, some analogues were also found to have the ability to decrease the expression level of HIF-1 alpha in breast cancer cells MDA-MB-231 under hypoxia. The features of these analogues suggest their potential in cancer therapy. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.12.032
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文献信息

  • Synthesis and biological activity of novel shikonin analogues
    作者:Wenjing Wang、Mei Dai、Caihua Zhu、Jiangang Zhang、Liping Lin、Jian Ding、Wenhu Duan
    DOI:10.1016/j.bmcl.2008.12.032
    日期:2009.2
    A series of shikonin analogues with side chain variants have been synthesized and evaluated for antitumor activity. These novel analogues show a broad spectrum of in vitro cytotoxicity against various cancer cell lines. Additionally, some analogues were also found to have the ability to decrease the expression level of HIF-1 alpha in breast cancer cells MDA-MB-231 under hypoxia. The features of these analogues suggest their potential in cancer therapy. (C) 2008 Elsevier Ltd. All rights reserved.
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